Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8294333 | Biochemical and Biophysical Research Communications | 2018 | 7 Pages |
Abstract
The recognition of single-stranded RNA by TLR7/8 leads to the production of NF-κB-mediated cytokines and type I IFNs. However, the role of TLR7/8 activation in monocytes and macrophages is still unclear. The aim of this study was to investigate the differences in the activation of TLR7/8 between these two cell types. Microarray analysis, qRT-PCR and flow cytometry were used to analyse TLR7/8 signalling pathways in monocytes and macrophages after stimulation with agonists. Our data indicated that TLR8 agonists activated the NF-κB- and IRF-mediated pathways in THP-1â¯cells, whereas TLR7 agonists did not. However, silent TLR8 and enhanced TLR7 expression could increase TLR7-induced NF-κB activation in monocytes. TLR7 and TLR8 agonists induced NF-κB activation but no ISG response in PMA-differentiated THP-1â¯cells. The mRNA levels of pro-inflammatory cytokine were elevated upon CL075 stimulation in macrophages compared to monocytes. Thus, TLR7 and TLR8 might modulate different immune responses in monocytes and macrophages.
Keywords
Interleukin-1 receptor-associated kinase 4IRAK1ISGTLR7AP-1IL-12p40IRAK4HEPESTLR8FBSIL-6IRF7cDNAComplementary DNAhydroxyethyl piperazineethanesulfonic acidinterferonIFNinterleukin 6Enzyme-linked immunosorbent assayELISAfetal bovine serumInterferon regulatory factor 7MacrophagesImmune modulationMonocytesactivator protein 1interleukin-1 receptor-associated kinase 1
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Biochemistry
Authors
Hock-Liew Eng, Yuan-Ying Hsu, Tsun-Mei Lin,